Canonical Allele Identifier: CA2374742984

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350461A= , CM000682.2:g.63350461A=	GRCh38
NC_000020.10:g.61981813A= , CM000682.1:g.61981813A=	GRCh37
NC_000020.9:g.61452257A=	NCBI36
NG_011931.1:g.15883T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.950T= MANE Select	ENSP00000359285.4:p.Val317=
ENST00000370263.8:c.950T=	ENSP00000359285.4:p.Val317=
ENST00000463705.5:n.1598T=
ENST00000467563.3:n.1020T=
ENST00000498043.6:c.974T=
ENST00000615287.4:c.737T=	ENSP00000483388.1:p.Val246=
ENST00000627000.1:c.*639T=	ENSP00000486914.1:n.*639T=
ENST00000630240.1:n.671T=
NM_000744.6:c.950T=	NP_000735.1:p.Val317=
NM_001256573.1:c.422T=	NP_001243502.1:p.Val141=
NR_046317.1:n.1206T=
XM_011528524.1:c.737T=	XP_011526826.1:p.Val246=
XM_017027625.2:c.422T=	XP_016883114.1:p.Val141=
XM_024451822.1:c.422T=	XP_024307590.1:p.Val141=
NM_001256573.2:c.422T=	NP_001243502.1:p.Val141=
NR_046317.2:n.1159T=
NM_000744.7:c.950T= MANE Select	NP_000735.1:p.Val317=